HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244635Erstellt: 23. Oktober 2026
Diisopropylethylamine → N-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamide
https://huagongshe.com/de/reaction/244635
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Methyl-1,3-thiazole-4-carboxylic acid | HCID 284728 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Edukt | 6-Bromo-1H-indazol-4-amine | HCID 24728063 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamide | HCID 58255750 | 18,9% |
Reaktionsschritte
2-Methyl-1,3-thiazole-4-carboxylic acid (4.59 g) (available from Maybridge), HATU (13.41 g) and DIPEA (16.80 ml) were stirred in DMF (140 ml) for 30 min at 20° C. 6-Bromo-1H-indazol-4-amine (3.4 g) (available from Sinova) was added and the reaction stirred at 20° C. for 2 days. The solvent was reduced to ˜40 ml and the reaction mixture was applied across 5×70 g aminopropyl SPE cartridges and left to stand for 3 h. The cartridges were eluted with DCM:methanol (1:1) and the combined solvent was evaporated in vacuo. The residue was suspended in DCM:methanol, adsorbed onto Florisil® and purified by chromatography on silica gel (100 g cartridge) eluting with 0-15% gradient of methanol (containing 1% triethylamine) in DCM over 60 min to give title compound (1.02 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08658635B2 |
|---|
| Quelldatensatz | uspto-grants-2014_02 |
|---|
| ORD ID | ord-a9afde083cea40e7829cf979ee997c21 |
|---|
| Quellennotiz | uspto-grants-2014_02 |
|---|